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White House Gives Go-ahead For Elitists to Control DNA

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Michael Edwards
Activist Post
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It is official: in the name of “clean energy, pollution control and medicine,” the White House is prepared to let scientists, spearheaded by the J. Craig Venter Institute, “manipulate DNA of organisms to forge new life forms,” according to a recent AFP article.

The Orwellian language used by Barack Obama’s Presidential Commission For The Study of Bioethical Issues is a study in wordiness, misdirection, and obfuscation that is typical when trying to cover up the true intent.  For example, on one hand the Commission acknowledges that the J. Craig Venter Institute has found the ability to forge new life forms, but also states that Venter’s team didn’t create life, since the work primarily involved altering an already existing life form. More

BABY DNA ALERT – The Baby DNA Warehouse bill (SF 1478)Minnesota

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BABY DNA ALERT – The Baby DNA Warehouse bill (SF 1478) may be announced last minute for Monday (3:00 p.m.) or for Tuesday (3:00 p.m.). The author is having another bill heard by the committee on Monday, and could conceivably do the baby DNA bill at the same time. Need MORE petitions to Governor
Contact your Representatives. Vote could come anytime in the House. (rep.firstname.lastname@house.mn) Find your legislator on the right side of our home page: http://www.cchconline.org


Citizens Line Up to Speak

CCHC “What Happened” REPORT
– click here for more photos

Crowd Challenges Health Department’s Medical Records Grab

Yesterday, in a room filled with people who came to comment on the Health Department’s medical record grab—and their planned use of the data to centralize treatment decisions and restrict access to care—the Department stalled the conversation.

State officials used up the first hour with department presentations. Meanwhile KSTP-TV waited for the action to begin. And waited. And waited.

After I asked them to provide their definition of health care “quality” (which they refused to answer), they cut off all audience questions until the end.

After they used up the first hour with three presentations, they asked every person to limit their comments to five minutes.

Engaged Audience:
The audience, most of them wearing CCHC “My Medical Records are Mine” stickers, was very engaged once the presentations were over, occasionally shouting out vocal rebuffs of less-than-transparent answers by the Department. They also applauded various comments made by the public.

MDH may be hoping no one ever hears about the meeting. They chose not to record attendance (no sign-in sheets) or to tape record the public’s comments.

Today we publish the CCHC report of the meeting, with lots of photos, to make sure the public knows what actually happened.

Coming soon…a YouTube video of a very impassioned and noisy exchange between one woman and the Health Department officials on the constitutionality of government taking private data.

Twila Brase
President, CCHC
651-646-8935

Minnesota Department of Health Continues to Store Baby DNA without Required

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MEDIA RELEASE
Wednesday, December 10, 2008
For Immediate Release



Minnesota Department of Health Continues to Store Baby DNA without Required

 

Parent Consent; Violates Genetic Privacy Law…and Governor’s Veto

 

 

CCHC calls on Governor Pawlenty to require compliance with state law

St. Paul/Minneapolis – In a press conference held today, concerned parents and the Citizens’ Council on Health Care (CCHC) called on Governor Tim Pawlenty to require his Commissioner of Health to cease and desist the warehousing of newborn blood and baby DNA without informed, written parent consent.

“Despite Governor Pawlenty’s veto of the health department’s DNA warehousing bill last legislative session…we have confirmed that the Minnesota Department of Health is continuing to warehouse baby DNA without parent consent. This is a direct violation of the genetic privacy and DNA property rights of parents and children,” said Twila Brase, president of CCHC.

DeEtta Moos, mother of four children, said, “Last session, there was an attempt to undercut Judge Neilson’s ruling, but thanks to Governor Pawlenty’s veto, the Minnesota Genetic Privacy Law still demands the requirement of parental consent for storage of blood and any purposes beyond the initial testing.”

Ryan Sibinski, expectant father of twins, expressed his disappointment saying, “My wife and I are acutely aware that storage of newborn DNA is still being done illegally by the MN Department of Health.  We thought the Governor’s veto was supposed to solve this, but we have now discovered that the storage continues.”

Mr. Sibinski continued, “In two months or less, our babies will be born. I request here today that the Department of Health make sure that I am clearly asked to consent to the storage, use, and sharing of my children’s blood and DNA.   This is my legal right under the law.”

Attorney Nathan Hansen, who has been attempting to obtain public documents regarding the transfer and use of newborn DNA for research studies, said, “No excuse has been given by the Department for this information not to be handed over.”

Notable History:

  • August 1, 2006 – Minnesota Genetic Privacy Law (M.S. 13.386) becomes effective. Informed written consent required for collection, storage, use and dissemination of genetic information by government and others.
  • January 23, 2007 – At request of concerned citizens, a public hearing was held on the health department’s proposed revision to the newborn screening rule.
  • March 23, 2007 – Administrative Law Judge (ALJ) Barbara Neilsen rules that the Minnesota Department of Health (MDH) is violating the 2006 state genetic privacy law’s informed written consent requirements for storage, use and dissemination.
  • July 3, 2007 – Chief Administrative Law Judge Raymond R. Krause denies Health Commissioner Dianne Mandernach’s appeal of the Neilsen ruling.
  • August 29, 2007 – Commissioner Mandernach withdraws the proposed revision to the newborn screening rule.
  • February 25, 2008 – Legislation introduced in the Minnesota legislature to exempt the newborn screening program (collection, storage, use, and dissemination) from the genetic privacy law’s requirements for informed, written consent.
  • May 19, 2008 – Governor vetoes S.F. 3138, prohibiting an exemption to the genetic privacy law’s consent requirements. He mentions ALJ ruling in his veto letter.
  • November 18, 2008 – David Orren, MDH Chief Legal Counsel, confirms to CCHC that MDH continues to store newborn blood without consent.

Ms. Brase called on Governor Pawlenty to act, saying, “We call on Governor Pawlenty to take immediate steps to assure the public that he supports the rule of law, and holds his administration accountable to follow the law. Let me suggest that he issue a statement today guaranteeing the health department’s compliance with the written informed consent requirements of the genetic privacy law. He could decree that no newborn blood be warehoused, used for research, or shared with others without informed written parent consent. He could order the health department to release public documents in compliance with the Government Data Practices Act. And he could also promise to dismantle the state’s DNA warehouse, protecting the genetic privacy rights of the more than 780,000 children whose DNA has been claimed by state government and warehoused without consent.”

-CCHC-

Links to the Governor’s veto letter, the Administrative Law Judge’s decision, the Minnesota Department of Health and CCHC documents can be found at http://www.itsmydna.org

Citizens’ Council on Health Care supports freedom for patients and doctors, medical
innovation, and the right to a confidential patient-doctor relationship.